Three-band phosphor for multi-layer agricultural plastic film

ABSTRACT

A blue-green-red three-band phosphor for multilayer agricultural plastic film for converting near ultraviolet light in photosynthetic active radiation is disclosed. The substrate of the phosphor is prepared from the group IIA element SiO 4   4− , having a total stoichiometric equation (ΣMe +2 O) 2α (SiO 2 ) α , in which α=1, 2, 3, ΣMe +2 =Ba +2  and/or Sr +2  and/or Ca +2  and/or Mg +2 , having an orthorhombic crystal architecture, and generating a three-band spectrum when activated by d-f element selected from the group of Eu +2 , Mn +2  and Sm +2 . The maximum wavelength of the three-band spectrum is λ 1 =440˜460 nm, λ 2 =515˜535 nm and λ 3 =626˜640 nm. The maximum value and halfwave width of every spectrum are determined subject to the concentration of the activator and the phosphor synthesis technology. The three-band phosphor is prepared through a solid synthesis method in the form of high dispersed ultrafine powder having the average grain size of d≦0.8 μm. The use of an agricultural plastic film made according to the present invention in an enclosed soil equipment greatly raises the productivity of vegetable crop.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to agricultural field and soil enclosure means for seasonal hot bed and greenhouse and more specifically, to the agricultural science and technology for creating optimal spectrum and sunlight illumination atmosphere for green plants under a seasonal thin-film covered hotbed condition.

2. Description of the Related Art

Since the foundation work of research by Russian natural scientist K. A. Timiriazev in 1896-1919, it has been for sure that sunlight is absorbed into the leaves of green plants by a green pigment, which absorbs red and blue light, but reflects green light, causing the leaves to appear green. This light energy is then converted into a chemical energy in the form of starch or sugar: 6CO₂+6H₂O→C₆H₁₂O₆+6O₂.

This equation translates as six molecules of water (6H₂O) plus six molecules of carbon dioxide (6CO₂) produce one molecule of sugar (C₆H₁₂O₆) plus six molecules of oxygen (O₂).

Since the creation of phosphor light source in 1930˜1950, all greenhouses and hotbed provide red and blue radiation light sources. Under the illumination of radiation light sources, the amount of vegetables and fruits obtained from the enclosed soil equipment is greatly increased. Solar radiation goes through a polyethylene thin film and the pigment of the polyethylene thin film is modified to, for example, light blue or rose. In the years of 1980˜1990, light conversion agricultural films were appeared. The radiation of these light conversion agricultural films include 5˜6% red light. This red light reacts with 6% original solar ultraviolet radiation. These agricultural films were patented in many countries around the world, such as Russian Patent 2160289 (inventor Soschin. N et. al.), Russian Patent 2064482 (inventor Soschin. N et. al.), U.S. Pat. No. 6,153,665 (inventor Goldburt et. al.), Euro Patent 999/35595 (inventor Bolschukxin W. et. al.), and Mexico Patent MX 01004165A (inventor E. T. Boldburt et. al.). The invention adopts the aforesaid patents as reference objects. In the aforesaid patents, a first generation light conversion agricultural plastic film utilizes Y₂O₂S:Eu based narrowband red phosphor, which has best conversion efficiency as known. The half-wave width of the spectrum band is smaller than 5 nm, assuring enhancement of red quantum concentration on the surface of green plants. Under the effect of light conversion agricultural plastic films, the production of vegetables and fruits in hotbed is increased by 20˜75%, and the nutrition composition of vegetables and fruits is substantially improved, for example, vitamin and minor element content of vegetables and fruits is increased.

Although the first generation light conversion agricultural plastic films have been intensively used for agricultural purposes, they still have drawbacks. At first, light conversion involves red spectrum region only, giving no effect on the second shortwave of blue spectrum. Under this condition, photosynthesis is periodically destroyed Further, reduction of transmissive light in blue and green spectrum regions of the light conversion agricultural plastic films results in extended growth period of greenhouse crop. The creation of a thin film having blue-red re-radiation characteristic eliminates a part of the aforesaid drawbacks. US2000/24343 (inventor Soschin. N. et. al.) discloses a similar design. The invention utilizes this invention as a prototype. The blue and red phosphors filled in this agricultural plastic film create supplementary light for plants. Using blue and red conversion radiator means in a film layer is a continuation and development of this concept, and has become a patent of France researchers (see WO 00/24243, inventor Blanc. W. et. al.). They created a single-component dual-band phosphor based on Ba₃MgSi₂O₈:Eu⁺²Mn⁺². With respect to the fabrication of agricultural plastic films, the concept of the aforesaid patent assures its advantages. However, in the literature, we did not find any strick proof of the applicability of this agricultural plastic film. The application of this dual-band phosphor may be constrained to its defect because photosynthesis requires all the three spectrum regions: blue, green and red at different radiation amounts.

Actually, according to data from modern researchers, spectrum illumination has the following physiological meanings: 1. 280˜320 nm UVB light will damage plants; 2. Radiation of UVB and near UVB light at a small amount has a great concern with growth regulation of plants; 3. Purple and blue light are requisite for photosynthesis and regulation of upper green leaves (plant root system); 4. Green and yellow radiation provides a long-lasting effect, and is partially absorbed by lush green leaves and dense tender branches of plants; 5. Orange and red radiation is necessarity for photosynthesis; 6. 700˜750 nm dark red radiation is the message communication path for green plants; and 8. 1200˜1600 nm infrared radiation heats and dissolves plants nutrients. From this short catalogue, we obtain the conclusion that full-spectrum illumination in radiation is necessary.

SUMMARY OF THE INVENTION

The present invention has been accomplished under the circumstances in view. It is the main object of the present invention to provide a three-band phosphor, which is practical for making a thin film light conversion material having the main spectrum at blue, green and red regions.

It is another object of the present invention to provide a three-band phosphor for multilayer agricultural plastic film, which is practical for making a material that exists in the form of an inorganic phosphor for radiation conversion in blue, green and red spectral regions subject to predetermined strength ratio.

To achieve these and other objects of the present invention, the three-band phosphor is based on the substrate of the group IIA element SiO₄ ⁴⁻ and activated by d-f element, characterized in that the three-band phosphor pertains to (MeO)_(2α)(SiO₂)_(α) silicate series, in which α=1, 2, 3, ΣMe⁺²=Ba⁺² and/or Sr⁺² and/or Ca⁺² and/or Mg⁺², having an orthohombic crystal architecture, and generating a three-band spectrum when activated by d-f element;

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

At first, the object of the present invention is to eliminate the drawbacks of the aforesaid conventional agricultural plastic film. A three-band phosphor in accordance with the present invention comprises a silicate-based substrate prepared from a group IIA element and activated by d-f element, characterized in that the three-band phosphor pertains to (MeO)_(2α)(SiO₂)_(α) silicate series, in which α=1, 2, 3, ΣMe⁺²=Ba⁺² and/or Sr⁺² and/or Ca⁺² and/or Mg⁺², having an orthohombic crystal architecture, and generating a three-band spectrum when activated by d-f element;

wherein the d-f element can be Eu⁺², Mn⁺² or Sm⁺²;

wherein the maximum wavelength of the three-band spectrum is λ₁=440˜460 nm, λ₂=515˜535 nm and λ₃=625˜650 nm;

wherein when α=1, the three-band phosphor has the stoichiometric equation of (Ba_(1.0)Sr_(0.30)Ca_(0.30)Mg_(0.4)) SiO₄, the activator of Eu⁺², Mn⁺² or Sm⁺² at the concentration of 0.001<Eu≦0.02, 0.0001<Sm≦0.005, 0.001<Mn≦0.015, and orthohombic crystal lattice structure capable of causing blue-green-red radiation in which the band relative intensity ratio is 1:0.5:1˜1:0.25:0.5;

wherein, when α=2, the three-band phosphor has the stoichiometric equation of (Ba_(0.5)Sr_(1.5)Ca_(1.0)Mg_(1.0))Si₂O₈:EuSmMn, an orthohombic crystal lattice structure, activator atomic fraction: 0.001≦Eu≦0.01, 0.0001≦Sm≦0.005 and 0.005≦Mn≦0.15, capable of having the three-band visible spectrum be within the blue-green-red zone when band strength ratio is 1:2:2˜1:2:4;

wherein, when α=2, the three-band phosphor has the stoichiometric equation of Ba_(0.25)Mg₁Sr_(1.75)Ca₁Si₂O₈, activator Eu⁺², Mn⁺² or Sm⁺², three-band visible spectrum in blue, green and red zones, and the band strength ratio of the three-band phosphor is 2:2:3 when activated by near ultraviolet light;

wherein the three-band phosphor is an ultrafine grinding powder of average powder grain size 0.4≦d_(cp)≦0.8 μm and variation range of specific surface 46·10³≦S≦80·10³ cm²;

wherein the three-band phosphor is an ultrafine grinding powder covered with lightproof pores of pore radius 12 A≦τ≦20 A, showing a ratio relationship between the powder surface and the pore surface of 10:1˜10:2.

The physical-chemical material properties of the three-band phosphor will be outlined hereinafter.

At the first place, these inorganic materials are linked by one single chemical formula. When the stoichiometric index α=1, the formula of this three-band phosphor is recorded as Me⁺² ₂Si₁O₄. When the stoichiometric index α=2, the formula of this three-band phosphor is recorded as Me⁺² ₄Si₂O₈. When the stoichiometric index α=3, the formula of this three-band phosphor is recorded as Me⁺² ₆Si₃O₁₂. At the second place, the composite provided by the present invention exits only in one type of atom, for example, Ba₂SiO₄ or Ba₄Si₂O₈. When cation content (atomic fraction) in crystal lattice is equal, the chemical formula of the composite provided according to the invention can be recorded as BaMgSiO₄ or (Ba,Mg,Sr,Ca)₄Si₂O₈. At the third place, the composite crystal of the present invention has mainly an orthorhombic crystal lattice structure in which the number of molecules per unit cell Z=4.

As stated in our research, the aforesaid composite can easily be activated by metallic ions, such as Sm⁺² (d-f element), Eu⁺² (d-f element) and Mn⁺² (d element), forming a stable solid solution. Under this activation effect, the phosphor emit light. When excited by shortwave light, it produces three (two is rare) emission bands, at blue, green and red radiation zones. At this time, the luminescent center of blue color is (Eu⁺² _(Me+2)), the luminescent center of red color is (Mn⁺² _(Me+2)), and the accurate record of the luminescent center of green color is unknown but the imaginated ideal luminescent center can be (Mg_(Ba))° or (Sr_(Ba))° or (Ca_(Ba))°. Small size IIA group cation Ba⁺² is formed in the composite crystal lattice during same valence isomorphous substitution.

Annexes I˜IV introduce radiation spectrum of phosphors prepared according to different embodiment of the present invention. In the spectrum of Annex I, first and second maximum values are obviously shown at λ=450 nm and λ=520 nm. A third maximum value appears at λ=626 nm but not so obvious. It is to be understood that the introduced spectra have concern with the composites (Ba_(0.5)Sr_(0.15)Ca_(0.15)Mg_(0.2))₂SiO₄:EuSmMn (see Annex I), (Ba_(0.8)Sr_(2.2)Ca_(0.5)Mg_(0.5))Si₂O₈:EuSmMn (see Annex II) and (Ba_(0.4)Sr_(4.6)Ca_(0.5)Mg_(0.5))Si₃O₁₂:EuSmMn (see Annex III). Actually, they show no any regular relationship relative to spectrum of the one pack phosphor Ba₃MgSi₂O₈:EuMnPr. Firstly, all the spectra have three maximum values but not two as indicated in the prototype module of the patent. Secondarily, all the spectra have different maximum strengths (in Annexes I & II, the shortwave is higher; in Annex III, the medium wave is higher; in Annex IV, the long wave is higher). Further, the half-wave width of every radiation varies with the composition of the phoror, for example, λ_(0.5)=60˜90 nm. A phosphor prepared according to the present invention has the important features of high quantum efficiency and high luminescence intensity.

A phosphor prepared according to the present invention has a high energy brightness value about 60·10³˜120·10³ energy units (as a comparison standard, phosphor sample Ba_(1.96)Eu_(0.04)SiO₄ has the energy brightness of L=80·10³ energy units). Realization of a phosphor having the said outstanding features according to the present invention is subject to the following conditions. The material has the stoichiometric formula (Ba_(1.0)Sr_(0.30)Ca_(0.30)Mg_(0.4))SiO₄, activators Eu⁺², Sm⁺² and Mn⁺² at concentration 0.001<Eu⁺²≦0.02, 0.0001<Sm⁺²≦0.005, 0.001<Mn⁺²≦0.015. The composite has a orthohomic crystal lattice architecture, assuring blue-green-red radiation. The band strength ratio is 1:0.5:1˜1:0.25:0.5. We see the phosphor has the maximum energy efficiency of radiation of L≧100·10³. This kind of radiat body is requisite for greenhouse equipment in culturing protein-rich crops such as soy bean and green pea.

Hereinafter, we explain the effect of each kind of cations in the radiation of a three-band phosphor prepared according to the present invention. At first, Ba⁺² enhances the lattice parameter of SiO₄ ⁴⁻, allowing accommodation of relatively bigger size of Eu⁺² (Eu⁺² ionic radius τ_(Eu)=1.24 A that is the largest in these cations). When compared with Ba⁺², Mg⁺² has the smallest ionic radius (τ_(Mg)=0.65 A), assuring high static gradient in the crystal lattice. This has a great concern with the characteristics of Mg⁺² that carries 2 units of charge and has a mall size. Further, Sr⁺² and Ca⁺² must be provided in the composition due to the following reasons: 1. In order to reduce the molecule mass of the stoichiometric equation of the phosphor provided according to the present invention, i.e., in order to reduce material consumption of the phosphor composition; 2. In order to form the geometric size of the non-equivalent weight luminescence center, the middle green radiation band must be extended as long as possible. Therefore, Sr⁺² is added to the crystal lattice to assure formation of the center of (Sr⁺² _(Ba+2)), more particular when (Sm⁺² _(Ba+2))° exists, it assures green-yellow luminance. This effect is produced by the isomorphic substitution of Ca⁺² in the SiO₄ ⁴⁻; 3. In order to form a uniform internal crystal medium, inducing a regulator effects between big size Ba⁺² and small size Mg⁺².

The aforesaid every ion formation provides a respective SiO₄ ⁴⁻ having a respective melting temperature, such as Mg₂SiO₄ T_(melting)=1450° C., Ca₂SiO₄ T_(melting)=1480° C., Sr₂SiO₄ T_(melting)=1350° C., Ba₂SiO₄ T_(melting)=1320° C.

When compared with the known prototype of the material of Ba₃MgSi₂O₈, the phosphor of the present invention has the feature of ecological safety. Because Ba⁺² is toxic, it must be constrained in the material. Similar to BaSO₄, indissolvable Ba⁺² nitrate, chloride and bromide are ecologically dangerous. Dissolvability data of Ba₃MgSi₂O₈ is not available in literatures. However, this compound is dissolvable in acid soil. Therefore, the concentration of Ba⁺² in the phosphor of the present invention must be reduced, and less toxic Ca⁺², Mg⁺² and Sr⁺² are used as substitutes. From this point of view, the composition of (Ba,Mg,Sr,Ca)Si₂O₈ has a great developed foreground. In this composition, the mass of Ba⁺² is reduced by 75% (cation lattice). From an ecological point of view, the composition of (Ba_(0.5)Sr_(1.5)Ca₁Mg₁).Si₂O₈:Eu⁺²Sm⁺²Mn⁺² in which the content of Ba ion mass is below 12%, has a better foreground. The phosphor of the present invention is characterized in that, the material has the stoichiometric equation (Ba_(0.5)Sr_(1.5)Ca_(1.0)Mg_(1.0))Si₂O₈:EuSmMn, an orthohombic architecture, and the activator: 0.001≦Eu≦0.01, 0.0001≦Sm≦0.005, 0.005≦Mn≦0.15, assuring blue-green-red three-band radiation in which the band relative intensity ratio is 1:2:2˜1:2:4.

As stated above, this phosphor is requisite in greenhouse facility for fruit cultivation. The strong red emmission peak of the radiation λ=630 nm assures high sugar content and good taste of the cultivated crops. It is to be understood that the three-band phosphor of the present invention shows substantial benefits in multilayer greenhouse radiation where plants are intensively cultivated. The green light of the conversion spectrum is working on seedlings and plants at the lower side, assuring the desired germination rate and proper growth.

As stated above, the three-band phosphor of the present invention has high brightness of luminous energy. At this time, the rest part is sufficiently uniformly distributed in all the spectrum λ=400˜800 nm. These outstanding benefits have a great concern with the inorganic three-band phosphor characterized in that: when α=2, the material has the stoichiometric equation of (Ba_(0.25)Sr_(1.75)Ca_(1.0)Mg_(1.0))Si₂O₈ and an orthohombic crystal lattice structure, activator Eu⁺², Sm⁺² or Mn⁺² of atomic fraction 0.001≦Eu⁺²≦0.05, 0.0004≦Sm⁺²≦0.01, 0.001≦Mn⁺²≦0.05: three-band visible spectrum in blue, green and red zones, and the band strength ratio of the three bands 2:2:3 when activated by violet light.

The substantial effect of the activator concentration in the phosphor substrate on the radiation strength of each band is described hereinafter. If the concentration of active ion Eu⁺² is 0.001<[Eu⁺²]≦0.01, the intensity of blue band radiation shows a linear relationship with the concentration of the added activator. The Eu⁺² supplement widens the spectrum bandwidth to λ_(0.5)=80 nm, enhancing the strength to 1.5˜2 units. To obtain high resolution spectral characteristics, [Mn⁺²] is added to the composite at 0.001≦[Mn⁺²]≦0.005. Starting from this maximum value, the radiation strength of manganese ion in red spectrum is J=0.2˜2.0. Red band strength extends to 0.018≦[Mn⁺²]≦0.02. Thereafter, the bandwidth is being widened, and the maximum value is shifted to the red zone of λ=625˜638 nm.

The more complicated condition is that the radiation strength of green band λ=520 nm is determined subject to [Sm⁺²] and the concentration ratio between the based ions, i.e., [Sr]/[Ba] and [Sr]/[Ca]. In the study, we emphasized the linear relationship when the concentration of the added ion was 0.0001≦[Sm⁺²]≦0.005. Thereafter, the substantial effect on the peak position was caused by [Sr⁺²] that was used to substitute for [Ba⁺²]. When [Sr⁺²]/[Ba⁺²]=4:1, the peak strength of green band was 1.5˜2 units, and no significant change was discovered when added [Ca⁺²]. Following increase of this cation in the phosphor substrate, the spectrum band width of green spectrum region was increased to λ_(0.5)=85˜90 nm. In order to create the proposed three-band phosphor of the invention, we studied professional synthesis techniques, including long time mixing of material, arrangement and fine compacting of prepared material in the crucible, heat treatment of material under a weak reduction air pressure and the follow-up acid-alkaline processing process and grinding in a planet-ball-grinder.

During theynsis of an inorganic phosphor in accordance with the present invention, reagents were selected from carbonate, oxalate, and hydroxylamine compound of barium, strontium, calcium and magnesium. For the reagents, the activator is preferably selected from Eu₂O₃ (99.99%) and Sm₂O₃ (99.95%). MnCO₃ (99.5%) can also be used. It is for sure that activator content has a great concern with the mass of the product prepared. Therefore, the content measurement error of the activator must not exceed by 5% of the mass itself. All the requisite ingredients were weighed and loaded in a professional mixer having fine zirconia grinding balls therein, and mixed for 30˜120 minutes at the speed of 120˜250 r.p.m.

Prepared materials were distributed in a 0.5 L or 0.75 L alundum crucible and compacted with pressure P=1 kgf/cm². The alundum crucible was then carried to a high thermal conductivity of SiC furnace and heated uniformly and rapidly at the speed of 6° C./minute. Through professional guide tubes, a gas mixture, for example, 1˜5% hydrogen and 99%˜95% nitrogen was added to the electric furnace. High purity gas was used during synthesis. During synthesis, gas exchange rate is 1˜2 L/minute. At the initial synthesis stage, temperature was increased at the speed of 2˜4° C./minute. The electric furnace was heated to the temperature about T=1100° C. for 0.5˜2 hours, and then increased to the temperature range of T=1250˜1400° C. for about 1˜5 hours. Thereafter, the temperature of the electric furnace was dropped to T=400° C., while the assigned reduction environment was still maintained in the furnace. Thereafter, the product was removed from the crucible for further processing.

In Example I of the preparation of the three-band phosphor in accordance with the present invention, mix:

CaCO₃: 0.3 M SrCO₃: 0.3 M BaCO₃: 1 M Mg(CO)₃Mg(OH)₂: 0.2 M SiO₂: 1 M Eu₂O₃: 0.005 M MnCO₃: 0.01 M Sm₂O₃: 0.003 M

The weighed reagents were mixed in the ceramic drum of a mixer into which 500 g of zirconia grinding balls were filled. The ceramic drum was rotated at 120 r.p.m. for two hours. Thereafter, the material was delivered to a professional alundum crucible and heated under a weak reduction environment. The material in the crucible was compacted to 1 kgf/cm². The crucible was then carried to a high thermal conductivity of SiC furnace and heated to the temperature level of T=1100° C. at the speed of 4° C./minute, and then kept at this temperature level for a period of τ=40 minutes. The electric furnace was filled with a gas mixture H₂:N₂=5:95. Thereafter, the temperature of the electric furnace was increased to T=1350° C. at the speed of 4° C./minute and kept at this temperature level for 120 minutes. Thereafter, the furnace was cooled down to 200° C. while the filling of the gas mixture was continued. The product was ground in the ceramic drum of a mixer for final processing. Thereafter, the product was dissolved with 1˜2% phosphoric acid solution for 8˜10 minutes. The product was rinsed to a neutral PH value, and then dried in a drying cabinet at temperature T=120° C. for 180 minutes. The well-dried product was filtered through a screen of 500 meshes, and optical technical parameters and dispersibility of the product were measured.

Measurement of optical technical parameters is to make sure of the relationship between the composition of the spectrum radiation and the maximum value of the spectrum, the calculation of the chromaticity coordinates and main radiation wavelength. The composition of (Ba_(0.5)Sr_(0.15)Ca_(0.15)Mg_(0.2))₂SiO₄ was measured to have the relationship of band ratio in the spectrum blue:green:red=1:0.5:0.5, the chromaticity coordinates x=0.2988 and y=0.3034, and the main wavelength λ_(d)=473 nm. The sample was measured to have the luminescence brightness B=17046 units, luminance value L>84·10³. The dispersed composition of the phosphor was measured through a professional laser diffraction meter as follows:

d₁₀ = 0.5 μm d₅₀ = 0.8 μm d_(cp) = 1.0 μm d₉₀ = 2.6 μm

average specific surface area S=44·10³ cm²/cm³. There is no common viewpoint on the relative parameter of dispersed composition of phosphor for agricultural plastic film. Some industrial companies provide phosphors having an average grain size of 6≦d_(cp)<10 μm and a specific surface area of S≦4000 cm²/g. According to the viewpoint of the present invention, these big-sized phosphors are not practical for fabrication of thin plastic films because the grain size of d˜10 μm simply matches with polymerized thin-film of concentration h=30 μm. Therefore, the production technique of the invention is to create a nanometer grade of dispersed powder, i.e., the grain size of the phosphor is reduced to the level below 1000 nm=1 μm. This nanometer grade of phosphor has the advantages of: 1. it is suitable for making a thinner film layer for agricultural plastic film; 2. it is suitable for making a thin-film layer of higher luminescence brightness; 3. it substantially improves the brightness uniformity of the luminescence film. The three-band phosphor of the present invention realizes these advantages, i.e., the three-band phosphor is a highly dispersed ultrafine nanometer grade powder having an average grain size 0.4≦d_(cp)≦1.0 μm, the range of specific surface area S=44·10³ cm²/cm³.

The three-band phosphor prepared according to the present invention has the powder surface covered with lightproof pores. When measured by BET method, the lightproof pores have the pore radius of 12 A≦d_(z)≦20 A, showing a ratio between the pore surface area and the powder surface area 1:10˜2:10. The formation of these lightproof pores on the surface of the phosphor is firstly discovered by the present invention. These lightproof pores constitute important and unit parameters of the phosphor. Firstly, these lightproof pores on the surface of the phosphor improve luminescence brightness of the phosphor and provide an optical path for the radiation from the powder material toward the material surface. Secondarily, the existence of these pores improves the adherence of the phosphor to the polymeric material, thereby enhancing the mechanical tensile strength of the thin film layer. As stated above, a polyethylene-based N158 agricultural plastic film has the tensile strength of E=15 kgf/cm². This polyethylene-based N158 agricultural plastic film has filled therein non-porous phosphor. In case the polyethylene-based N158 agricultural plastic film has filled therein porous phosphor of the present invention, the tensile strength will be increased to E=30 kgf/cm². This is an important advantage of the phosphor of the present invention. The phosphor is characterized by that the ultrafine phosphor is covered with lightproof pores having the pore radius of 12 A≦d_(z)≦20 A, having the specific value between the powder surface area and the pore surface area 10:1˜10:2.

As indicated above, using a light conversion agricultural plastic film raises crop productivity by 20˜75%. In north hemisphere 20˜40° N, under long period solar radiation and windy conditions, we made a test on a three-band agricultural plastic film and three-band phosphor prepared according to the present invention. We selected eggplant and tomato as “test samples”. During a 49-day test period, the productivity of eggplant in the greenhouse was increased by 52% and the average eggplant mass per plant was 610 g compared to the eggplant mass per plant of 380 g during the same period; the productivity of tomato in the greenhouse was increased by 40% and the tomato mass per plant was increased by 5˜8%.

In conclusion, the three-band phosphor for agricultural plastic film in accordance with the present invention has the characteristics of: 1. practical for making a thin-film spectral conversion material having the main spectrum at blue, green and red zones; 2. practical for making a material in the form of an inorganic phosphor for converting radiation at blue, green and red spectral regions in conformity with a predetermined strength ratio, thereby eliminating the drawbacks of conventional agricultural plastic films.

Although particular embodiments of the invention have been described in detail for purposes of illustration, various modifications and enhancements may be made without departing from the spirit and scope of the invention. 

1. A three-band phosphor for agricultural plastic film, comprising a silicate-based substrate prepared from a group IIA element and activated by d-f element, wherein the three-band phosphor pertains to (MeO)_(2α)(SiO₂)_(α) silicate series, in which α=1, 2, 3, ΣMe⁺²=Ba⁺² and/or Sr⁺² and/or Ca⁺² and/or Mg⁺², having an orthohombic crystal architecture, and generating a three-band spectrum when activated by d-f element.
 2. The three-band phosphor as claimed in claim 1, wherein said d-f element is selected from the group of Eu⁺², Mn⁺² and Sm⁺².
 3. The three-band phosphor as claimed in claim 1, wherein the maximum wavelength of the three-band spectrum is λ₁=440˜460 nm, λ₂=515˜535 nm and λ₃=626˜640 nm.
 4. The three-band phosphor as claimed in claim 1, which has the stoichiometric equation of (Ba_(1.0)Sr_(0.30)Ca_(0.30)Mg_(0.4))SiO₄, the activator of Eu⁺², Mn⁺² or Sm⁺² at the concentration of 0.001<Eu^(≦2)=0.02, 0.0001<Sm⁺²≦0.005, 0.001<Mn⁺²≦0.015, and the orthohombic crystal architecture of the composite being able to cause blue-green-red radiation in which the band relative intensity ratio is 1:0.5:1˜1:0.25:0.5.
 5. The three-band phosphor as claimed in claim 1, which has the stoichiometric equation of (Ba_(0.5)Sr_(1.5)Ca_(1.0)Mg_(1.0))Si₂O₈:EuSmMn, an orthohombic crystal lattice structure, activator atomic fraction: 0.001≦Eu≦0.01, 0.0001≦Sm≦0.005 and 0.005≦Mn≦0.15, capable of having the three-band visible spectrum be within the blue-green-red zone when band strength ratio is 1:2:2˜1:2:4.
 6. The three-band phosphor as claimed in claim 1, wherein when α=1, the three-band phosphor has the stoichiometric equation of (Ba_(1.0)Sr_(0.30)Ca_(0.30)Mg_(0.4))SiO₄, the activator of Eu⁺², Mn⁺² or Sm⁺² at the concentration of 0.001<Eu≦0.02, 0.0001<Sm≦0.005, 0.001<Mn≦0.015, and orthohombic crystal lattice structure capable of causing blue-green-red radiation in which the band relative intensity ratio is 1:0.5:1˜1:0.25:0.5.
 7. The three-band phosphor as claimed in claim 1, wherein, when α=2, the three-band phosphor has the stoichiometric equation of Ba_(0.25)Mg₁Sr_(1.75)Ca₁Si₂O₈, an orthohombic crystal lattice structure, activator Eu⁺², Mn⁺² or Sm⁺², three-band visible spectrum in blue, green and red zones, and the band strength ratio of 2:2:3 when activated by near ultraviolet light.
 8. The three-band phosphor as claimed in claim 1, which is a highly dispersed ultrafine powder having an average powder grain size 0.4≦d_(cp)≦0.8 μm and variation range of specific surface 46·10²≦S≦80·10³ cm².
 9. The three-band phosphor as claimed in claim 8, wherein the three-band phosphor is an ultrafine grinding powder covered with lightproof pores having a pore radius 12 A≦τ≦20 A, showing a ratio relationship between the powder surface and the pore surface of 10:1˜10:2. 